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COL4A3 Gene Alport Syndrome Autosomal Recessive Genetic Test

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The COL4A3 gene plays a critical role in the structure and function of the kidneys, eyes, and ears. Mutations in this gene are associated with Alport Syndrome, a genetic disorder characterized by progressive kidney disease, hearing loss, and eye abnormalities. Alport Syndrome can follow different inheritance patterns, including autosomal recessive, where the individual must inherit two copies of the mutated gene, one from each parent, to be affected.

DNA Labs UAE offers a genetic test specifically designed to identify mutations in the COL4A3 gene that are linked to the autosomal recessive form of Alport Syndrome. This test is crucial for early diagnosis, which can significantly impact the management and prognosis of the condition. By analyzing an individual’s DNA, the test can confirm a suspected diagnosis, help in the assessment of disease progression, and guide treatment decisions.

The cost of the COL4A3 Gene Alport Syndrome Autosomal Recessive Genetic Test at DNA Labs UAE is 4400 AED. This comprehensive testing service provides valuable information for affected individuals and their families, enabling them to understand their genetic risk and consider appropriate preventive measures or treatments. It’s an important resource for those with a family history of Alport Syndrome or healthcare providers looking for a precise diagnosis to tailor patient care effectively.

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COL4A3 Gene Alport Syndrome Autosomal Recessive Genetic Test

Test Name: COL4A3 Gene Alport syndrome autosomal recessive Genetic Test

Components: COL4A3 gene analysis

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test type: Hepatology, Nephrology, Endocrinology Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for COL4A3 Gene Alport syndrome, autosomal recessive NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with COL4A3 Gene Alport syndrome, autosomal recessive NGS Genetic DNA Test gene COL4A3

Test Details

The COL4A3 gene is associated with Alport syndrome, which is a genetic disorder that affects the kidneys, ears, and eyes. This syndrome can be inherited in an autosomal recessive manner, meaning that both copies of the gene must be mutated for the individual to develop the condition.

NGS (Next-Generation Sequencing) is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including COL4A3. This technology can identify mutations or variations in the COL4A3 gene that may be responsible for causing Alport syndrome.

By performing an NGS genetic test, healthcare professionals can detect mutations in the COL4A3 gene and provide a diagnosis for Alport syndrome. This information is crucial for understanding the underlying cause of the condition and for guiding appropriate management and treatment strategies.

Test Name COL4A3 Gene Alport syndrome autosomal recessive Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Hepatology Nephrology Endocrinology Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for COL4A3 Gene Alport syndrome, autosomal recessive NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with COL4A3 Gene Alport syndrome, autosomal recessive NGS Genetic DNA Test gene COL4A3
Test Details

The COL4A3 gene is associated with Alport syndrome, which is a genetic disorder that affects the kidneys, ears, and eyes. This syndrome can be inherited in an autosomal recessive manner, meaning that both copies of the gene must be mutated for the individual to develop the condition.

NGS (Next-Generation Sequencing) is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including COL4A3. This technology can identify mutations or variations in the COL4A3 gene that may be responsible for causing Alport syndrome.

By performing an NGS genetic test, healthcare professionals can detect mutations in the COL4A3 gene and provide a diagnosis for Alport syndrome. This information is crucial for understanding the underlying cause of the condition and for guiding appropriate management and treatment strategies.